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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Bioeng. Biotechnol.</journal-id>
<journal-title>Frontiers in Bioengineering and Biotechnology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Bioeng. Biotechnol.</abbrev-journal-title>
<issn pub-type="epub">2296-4185</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">1192524</article-id>
<article-id pub-id-type="doi">10.3389/fbioe.2023.1192524</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Bioengineering and Biotechnology</subject>
<subj-group>
<subject>Systematic Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Understanding foot conditions, morphologies and functions in children: a current review</article-title>
<alt-title alt-title-type="left-running-head">Jiang et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fbioe.2023.1192524">10.3389/fbioe.2023.1192524</ext-link>
</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Jiang</surname>
<given-names>Hanhui</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2307283/overview"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Mei</surname>
<given-names>Qichang</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/644283/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wang</surname>
<given-names>Yuan</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/2297855/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>He</surname>
<given-names>Junhao</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Shao</surname>
<given-names>Enze</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1744002/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Fernandez</surname>
<given-names>Justin</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1440886/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Gu</surname>
<given-names>Yaodong</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<uri xlink:href="https://loop.frontiersin.org/people/505995/overview"/>
</contrib>
</contrib-group>
<aff id="aff1">
<sup>1</sup>
<institution>Faculty of Sports Science</institution>, <institution>Ningbo University</institution>, <addr-line>Ningbo</addr-line>, <country>China</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Research Academy of Grand Health</institution>, <institution>Ningbo University</institution>, <addr-line>Ningbo</addr-line>, <country>China</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Auckland Bioengineering Institute</institution>, <institution>The University of Auckland</institution>, <addr-line>Auckland</addr-line>, <country>New Zealand</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Department of Engineering Science</institution>, <institution>The University of Auckland</institution>, <addr-line>Auckland</addr-line>, <country>New Zealand</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1255274/overview">Claudio Belvedere</ext-link>, Rizzoli Orthopedic Institute (IRCCS), Italy</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/313803/overview">Redha Taiar</ext-link>, Universit&#xe9; de Reims Champagne-Ardenne, France</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/542334/overview">Elbe De Villiers</ext-link>, Stellenbosch University, South Africa</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Qichang Mei, <email>meiqichang@nbu.edu.cn</email>, <email>qmei907@aucklanduni.ac.nz</email>
</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>19</day>
<month>07</month>
<year>2023</year>
</pub-date>
<pub-date pub-type="collection">
<year>2023</year>
</pub-date>
<volume>11</volume>
<elocation-id>1192524</elocation-id>
<history>
<date date-type="received">
<day>04</day>
<month>04</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>12</day>
<month>07</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2023 Jiang, Mei, Wang, He, Shao, Fernandez and Gu.</copyright-statement>
<copyright-year>2023</copyright-year>
<copyright-holder>Jiang, Mei, Wang, He, Shao, Fernandez and Gu</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>This study provided a comprehensive updated review of the biological aspects of children foot morphology across different ages, sex, and weight, aiming to reveal the patterns of normal and pathological changes in children feet during growth and development. This review article comprised 25 papers in total that satisfied the screening standards. The aim was to investigate how weight changes, age and sex affect foot type, and gain a deeper understanding of the prevalent foot deformities that occur during children growth. Three different foot morphological conditions were discussed, specifically including the effect of sex and age differences, the effect of weight changes, and abnormal foot morphologies commonly documented during growth. This review found that sex, age, and weight changes would affect foot size, bony structure, foot posture, and plantar pressures during child growth. As a result of this biological nature, the children&#x2019;s feet generally exhibit neutral and internally rotated foot postures, which frequently lead to abnormal foot morphologies (e.g., flat foot, pronated foot, etc.). In the future, attention shall be paid to the causal factors leading to specific foot morphologies during the growth and development of children. However, sufficient evidence could not be provided due to a relatively short period of investigation and non-uniformed research methodology in the current literature. A more comprehensive and in-depth exploration is recommended to provide scientific evidence for the discovery of children foot development and personalized growth pattern.</p>
</abstract>
<kwd-group>
<kwd>children</kwd>
<kwd>foot morphology</kwd>
<kwd>foot posture</kwd>
<kwd>obesity</kwd>
<kwd>flatfoot</kwd>
<kwd>pes cavus</kwd>
</kwd-group>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Biomechanics</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1">
<title>Introduction</title>
<p>The human foot, consisting of a total of 26 bones, is one of the most significant parts of the human body (<xref ref-type="bibr" rid="B45">Mauch et al., 2009</xref>) and crucial for locomotion. Foot bones and relevant muscles, ligaments, and tendons played significant roles in preserving the general form and ensured functions under static or dynamic conditions (<xref ref-type="bibr" rid="B45">Mauch et al., 2009</xref>). In general, the foot is the first to grow during early childhood (<xref ref-type="bibr" rid="B12">Bosch et al., 2009</xref>). According to the growth of the foot stopped first, followed by the long bones (the femur and tibia), and lastly the body (<xref ref-type="bibr" rid="B45">Mauch et al., 2009</xref>). Reported that the biological performance of the foot in healthy children varied with age (<xref ref-type="bibr" rid="B44">Manousaki et al., 2019</xref>). It was discovered that foot width decreased with growing foot length as a normalization of the foot width to length, and adjusting for proportional variations during foot development (<xref ref-type="bibr" rid="B14">Bruner et al., 2009</xref>).</p>
<p>As children grow, the foot morphology varied between sex as well. As reported in several studies (<xref ref-type="bibr" rid="B21">Cheng et al., 1997</xref>; <xref ref-type="bibr" rid="B26">El et al., 2006</xref>; <xref ref-type="bibr" rid="B14">Bruner et al., 2009</xref>; <xref ref-type="bibr" rid="B48">Muller et al., 2012</xref>; <xref ref-type="bibr" rid="B71">Waseda et al., 2014</xref>; <xref ref-type="bibr" rid="B44">Manousaki et al., 2019</xref>), the foot length (FL) of boys increased until at least the period of 15&#xa0;years old, but girls showed scare increases beyond the period of 13&#xa0;years old. The navicular height (NH) of the boy&#x2019;s foot exhibited a gradual increase starting at the at 12, followed by a rapid rise at 13, and eventually reached a plateau at 15. In contrast, females&#x2019; NH rose gradually at 10, then quickly at 11, and finally hit a plateau at 16<sup>9</sup>.</p>
<p>Weight fluctuations could affect foot morphology, in addition to other variables, such as age, sex, and height. In many developed nations, child obesity is currently at &#x201c;epidemic&#x201d; levels (<xref ref-type="bibr" rid="B53">Racette et al., 2003</xref>). For public health services across the world, obesity has become an increasing burden and worry for public health services across the world, which is a condition becoming more common, showing long-term medical and social effects (<xref ref-type="bibr" rid="B70">Wang and Lobstein, 2006</xref>). Overweight and obesity, according to the World Health Organization, are abnormal or excessive fat deposits that affect general health. Overweight is defined as a body mass index (BMI) for the age that is one standard deviation over the median of the WHO growth reference criteria for school-age children and adolescents (5&#x2013;19&#xa0;years). Obesity (<xref ref-type="bibr" rid="B24">de Onis et al., 2010</xref>) was defined as a BMI for the age that was more than two standard deviations over the WHO growth reference criterion median. Being overweight put more strain on the musculoskeletal system as kids get older, which could affect their mobility, level of physical activity, and ability to carry out age-appropriate daily tasks. Obesity could cause musculoskeletal discomfort in various body regions (<xref ref-type="bibr" rid="B39">Krul et al., 2009</xref>). In addition to musculoskeletal pain and discomfort, being overweight or obese also led to orthopedic issues in the foot and ankle, knee, hip, and spine (<xref ref-type="bibr" rid="B32">Frey and Zamora, 2007</xref>; <xref ref-type="bibr" rid="B63">Stovitz et al., 2008</xref>). Additionally, this change significantly raised the chance of fractures, growth issues, and developmental problems (<xref ref-type="bibr" rid="B49">Must and Strauss, 1999</xref>; <xref ref-type="bibr" rid="B66">Taylor et al., 2006</xref>). Being overweight resulted in improper plantar pressure distribution, foot anatomical changes, and foot balance issues (<xref ref-type="bibr" rid="B31">Fink et al., 2019</xref>; <xref ref-type="bibr" rid="B50">Park and Park, 2019</xref>). Reduced flexibility from the changed foot anatomy stopped children from running or walking activities (<xref ref-type="bibr" rid="B49">Must and Strauss, 1999</xref>; <xref ref-type="bibr" rid="B66">Taylor et al., 2006</xref>; <xref ref-type="bibr" rid="B31">Fink et al., 2019</xref>; <xref ref-type="bibr" rid="B50">Park and Park, 2019</xref>). Additionally, being overweight could affect the plantar arch by affecting the bone and ligament support and causing the medial longitudinal arch to collapse (<xref ref-type="bibr" rid="B15">Buldt et al., 2018</xref>). Flatfoot was one of the most often reported problems, according to various studies, that such change in the arch may result in related foot conditions (<xref ref-type="bibr" rid="B57">Sachithanandam and Joseph, 1995</xref>; <xref ref-type="bibr" rid="B20">Chen et al., 2013</xref>; <xref ref-type="bibr" rid="B67">Telfer and Bigham, 2019</xref>). However, the two were not discovered to be associated, indicating that there was no connection between obesity and flat feet, in a later set of investigations on weight change and flat feet (<xref ref-type="bibr" rid="B60">Song-Hua et al., 2017</xref>).</p>
<p>Flatfoot in quite common in children, and the prevalence was determined by several variables, and the predisposing factors are not only obesity (<xref ref-type="bibr" rid="B2">Abolarin et al., 2011</xref>). The prevalence of flat feet may decrease as individuals age (<xref ref-type="bibr" rid="B54">Rao and Joseph, 1992</xref>). People who had pes planus (flatfoot) typically exhibited midfoot pronation or hindfoot valgus. Pes planus is a condition in which the medial longitudinal arch (MLA) collapses with the midfoot touching the ground entirely or almost completely (<xref ref-type="bibr" rid="B41">LeGuern et al., 1997</xref>; <xref ref-type="bibr" rid="B51">Pfeiffer et al., 2006</xref>). The opposite of flatfoot is a pes cavus (high-arched foot), which would not drop with weight bearing. It is typically a deformity because of muscular imbalance, which may be skeletal or soft tissue, or both combined. The deformity is primarily located in the hindfoot, forefoot (midfoot and forefoot), or a combination of both, with varying degrees of severity. According to <xref ref-type="bibr" rid="B78">Zimon et al. (2011)</xref> the Charcot-Marie-Tooth (CMT) disease was responsible for half of the pes cavus (<xref ref-type="bibr" rid="B13">Brewerton et al., 1963</xref>). Research investigating the timing and progression of foot and ankle changes in children with CMT, as a genetic condition affecting the peripheral nervous system and worsens over time, revealed that approximately 1 in 2,500 individuals was affected by this condition. The weakening of the distal lower extremity, causing foot drop, sensory loss, lacking tendon reflection, muscular spasms, and inverted foot deformity was the typical symptom of CMT (<xref ref-type="bibr" rid="B59">Skre, 1974</xref>; <xref ref-type="bibr" rid="B16">Burns et al., 2009</xref>). These symptoms resulted in several functional deficits, such as foot discomfort, ankle instability, tripping, falling, poor balance, and foot pain, which would affect gait performance (<xref ref-type="bibr" rid="B55">Redmond et al., 2008a</xref>; <xref ref-type="bibr" rid="B30">Ferrarin et al., 2012</xref>; <xref ref-type="bibr" rid="B23">Dars et al., 2018</xref>). One major symptom was the arch deformity (<xref ref-type="bibr" rid="B41">LeGuern et al., 1997</xref>; <xref ref-type="bibr" rid="B77">Zambito et al., 2008</xref>), but not always presenting in children. Clinical study, involving 32 children diagnosed with CMT and ranging in age from 7&#xa0;months to 15&#xa0;years, reported that 72% exhibited bilateral high arches, while 13% had flat feet (<xref ref-type="bibr" rid="B33">Ghanem et al., 1996</xref>; <xref ref-type="bibr" rid="B74">Wines et al., 2005</xref>). The result reflected that arch disorders could affect foot morphology.</p>
<p>However, whether increased weight in children could increase the risk of flatfoot disease and the causation of specific foot morphology is unknown. The answer to this question has been controversial, and this study is aimed to discuss the effects of age, weight, and sex differences on foot morphology and focuses on the patterns of abnormal foot changes. The existing studies are still unable to provide sufficient evidence due to factors such as short study periods and non-uniformed research methodology. Therefore, the goal of this review study is to investigate the influence of sex, change in age and weight, and the causal factors leading to abnormal foot morphology. Knowledge could provide a scientific basis for children&#x2019;s growth and development and the discovery of individualized growth patterns for clinical diagnosis.</p>
</sec>
<sec sec-type="materials|methods" id="s2">
<title>Materials and methods</title>
<p>The study focused on foot morphology changes in children, to discuss the normal and abnormal foot morphologies, thus summarizing the effect of sex, age, and weight differences on foot morphology, especially changes of flatfoot and high-arch foot in the midfoot. The range of this study was set at 0&#x2013;18&#xa0;years old according to the growth cycle of the children foot morphology (<xref ref-type="bibr" rid="B12">Bosch et al., 2009</xref>; <xref ref-type="bibr" rid="B14">Bruner et al., 2009</xref>; <xref ref-type="bibr" rid="B45">Mauch et al., 2009</xref>; <xref ref-type="bibr" rid="B71">Waseda et al., 2014</xref>; <xref ref-type="bibr" rid="B44">Manousaki et al., 2019</xref>), and foot changes caused by genetic or other diseases were excluded in the study. The review did not include data on human rights violations as contained in the Declaration of Helsinki, so ethics committee approval was not required.</p>
<sec id="s2-1">
<title>Search strategy</title>
<p>Researchers used databases, including PubMed, Web of Science, and Google Scholar, to conduct a comprehensive literature search strategy. Since our study focused on changes in foot morphology during child development, each search string had to contain the following key words, &#x2018;Children&#x2019;s feet&#x2019; and &#x2018;Morphology&#x2019;. Therefore, the following key phrases were retrieved using Boolean search syntax, [(Children&#x2019;s foot) OR (Children&#x2019;s feet)] AND [(morphology) OR (shape) OR (foot posture)] AND (age) AND (sex), with 134 documents found; [(Children foot) OR (Children feet)] AND [(morphology) OR (shape) OR (foot posture)] AND (foot (Children foot) OR (Children feet) AND [(morphology) OR (shape) OR (foot posture)] AND [(obesity) OR (overweight)], 112 searches [(Children foot) OR (Children feet)] AND [(morphology) OR (shape) OR (foot posture)] AND [(flat foot) OR (Pes cavus) OR (CMT) OR (Foot Valgus)]. Thus, a total of 207 articles were found. The search was not limited to the publication year. Studies released before January 2023 were included. A total of 453 uncensored duplicates were considered for topics, abstracts, and keywords. All copies were removed using reference software (Endnote) and manually checked by the Investigators (HJ, QM, and YG) before the literature screening.</p>
</sec>
<sec id="s2-2">
<title>Inclusion and exclusion criteria</title>
<p>The screening conditions followed the framework construction method of (<xref ref-type="bibr" rid="B42">Linares-Espinos et al., 2018</xref>) and the Preferred Reporting Items for Systematic Evaluation and Meta-Analysis (PRISMA) guidelines (<xref ref-type="bibr" rid="B47">Moher et al., 2009</xref>).</p>
<p>Inclusion: (1) the language of study is English; 2) young children, children, and adolescents; 0&#x2013;1&#xa0;years of age; sample size &#x3e;1; 3) studies focus on changes in foot morphology; prospective or retrospective studies involved at least changes in foot biomechanics or biological features; abnormal foot type studies should be about the characteristics of morphological changes and injury risk, biological features, plantar pressure; 4) studies should focus on tracer changes over time.</p>
<p>Exclusions: 1) congenital foot disease; other diseases causing foot changes; 18&#xa0;years of age or beyond; 2) foot has undergone surgery; 3) studies that (apparently) published duplicate results from the same subject sample as in previous publications obtained from the same group; biological feature values reported in the first study were excluded; 4) non-original articles (e.g., comments or conference articles); non-English articles; review; and 5) did not address foot biological features.</p>
</sec>
</sec>
<sec id="s3">
<title>Research risks</title>
<p>Although defining the age range of children between 0 and 18&#xa0;years, there were still individual differences in studies and even external factors such as race, region, and environment that may affect foot changes. <xref ref-type="table" rid="T1">Table 1</xref>.</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Inclusion and exclusion criteria.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center"/>
<th align="center">Inclusion</th>
<th align="center">Exclusion</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">Research direction</td>
<td align="center">(1) Studies in the English language; (2) Studies should focus on foot morphological changes; Prospective or retrospective studies at least involve changes in foot biomechanics or biological characteristics. In the study of abnormal foot form, the change characteristics relating injury risk to at least one biological characteristic, or plantar pressure; (3) Studies should focus on the tracking of changes in time</td>
<td align="center">(1) The foot has undergone surgery; (2) Studies (apparently) published duplicate results from the same subject sample, the same results in previous publications obtained from the same group; biological features reported in the first study were excluded; (3) non-original articles (e.g., comments or conference articles); non-English articles; review; (4) no biological features of the foot</td>
</tr>
<tr>
<td align="center">Subjects and age</td>
<td align="center">children and adolescents; 0&#x2013;18&#xa0;years old; sample size&#x3e; 1</td>
<td align="center">Congenital foot disease; Other diseases lead to foot changes; Over 18&#xa0;years old</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec sec-type="results" id="s4">
<title>Result</title>
<sec id="s4-1">
<title>Search results</title>
<p>The preliminary search data was 453 articles, and after deleting duplicates, the search yielded 238 articles. Among them, there were 64 articles about sex and age changes in children&#x2019;s feet. There were 52 articles on changes in the foot due to obesity and overweight. There were 122 articles on changes in specific foot types in children. After removing 100 articles from the keyword filtering in titles and abstracts; 32 studies with congenital foot disorders were excluded; 20 studies with other diseases causing foot changes were excluded; 9 studies with feet undergoing surgical treatment were excluded; 24 studies without foot biology were excluded; and 7 studies without foot morphology were excluded. Therefore, based on the screening eligibility criteria, a total of 32 studies were included for full-text screening. However, 3 studies did not meet the number of participants, 3 conference papers or reviews were excluded, and 1 study was retracted. Finally, 25 papers were found that satisfied the requirements for inclusion. <xref ref-type="fig" rid="F1">Figure 1</xref> illustrates the systematic search and selection process of the studies in detail.</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Illustration of literature search and selection process for the current study.</p>
</caption>
<graphic xlink:href="fbioe-11-1192524-g001.tif"/>
</fig>
</sec>
<sec id="s4-2">
<title>Flat foot</title>
<p>The flattened MLA, showing that the foot type had smaller arch angle as well as greater CSI and SI factor volume, was the primary attribute of the flat foot. The typical z-value for the foot length was around &#x2212;0.1 <sup>51</sup>.</p>
<p>The findings from <xref ref-type="table" rid="T2">Table 2</xref> showed that variations in skeletal architecture, foot posture, and plantar pressure distribution were influenced by differences in sex and age. These variations continued until maturity. Studies on infant foot posture have shown that boys often had flatter feet and lower arches than girls. With increasing age, 46.7% of children aged 8&#x2013;10 years had neutral feet and 53.3% had medially rotated feet (<xref ref-type="bibr" rid="B4">Al Kaissi et al., 2016</xref>). 56.9% of children aged 11 to 13 had neutral feet, 39.7% had medially rotated feet, and 3.4% had posteriorly rotated feet (<xref ref-type="bibr" rid="B4">Al Kaissi et al., 2016</xref>).</p>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Influence of Age and Sex on Foot type Changes</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">References</th>
<th align="center">Participants</th>
<th align="center">Sex</th>
<th align="center">Age</th>
<th align="center">Method</th>
<th align="center">Sex result</th>
<th align="center">Age result</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">
<xref ref-type="bibr" rid="B7">Ana et al. (2017)</xref>
</td>
<td align="center">2569</td>
<td align="center">1291 girls and 1278 boys</td>
<td align="center">9-15</td>
<td align="center">Researchers compiled data on children&#x27;s age distribution and mean bilateral FPI-6 scores.</td>
<td align="center">Males typically scored higher than girls did, and the left foot&#x27;s FPI-6 score was substantially greater than the right foot&#x27;s (p &#x3c; 0.05).</td>
<td align="center">The typical FPI-6 score for children and adolescents between the ages of 9 and 15 is 3.0-3.4, with neutral to slightly pronated foot morphology.</td>
</tr>
<tr>
<td align="center">
<xref ref-type="bibr" rid="B4">Al Kaissi et al. (2016)</xref>
</td>
<td align="center">150</td>
<td align="center">71 girls and 79 boys</td>
<td align="center">8-13</td>
<td align="center">Determined BMI, weight, FPI and height in the bipedal, static, and relaxed position.</td>
<td align="center">As compared to boys, a somewhat higher percentage of girls had pronated feet.</td>
<td align="center">Children aged 8 to 10 had neutral feet in 46.7 percent of cases and pronated feet in 53.3 percent. 11.9% neutral, 39.7% pronation, and 3.4% pronation were seen in children aged 11 to 13.</td>
</tr>
<tr>
<td align="center">
<xref ref-type="bibr" rid="B25">Delgado-Abellan et al. (2014)</xref>
</td>
<td align="center">1031</td>
<td align="center">534 girls and 497 boys</td>
<td align="center">6-12</td>
<td align="center">Measuring the barefoot condition. The boy or girl stood with both feet stilly with equally distributed weight on both feet during measurement.</td>
<td align="center">The aged with the largest sex difference was 8 - 9 years old and 9 - 10 years old. Boys&#x27; feet were wider than girls&#x27; feet, and the most significant differences between boys and girls of the same age were in ball width, ball circumference, and instep height.</td>
<td align="center">Through all ages evaluated the disparities in foot length increased linearly with height.</td>
</tr>
<tr>
<td align="center">
<xref ref-type="bibr" rid="B61">Stavlas et al. (2005)</xref>
</td>
<td align="center">5866</td>
<td align="center">2931 girls and 2935 boys</td>
<td align="center">6-17</td>
<td align="center">The Harris and Beath foot printing mat was used to obtain dynamic (walking) bilateral footprints in every child</td>
<td align="center">At the age of 7, 9, 11, 14 and 15, boys have a significantly higher proportion of low arch than girls of the same age</td>
<td align="center">No systematic description</td>
</tr>
<tr>
<td align="center">(<xref ref-type="bibr" rid="B76">Xu et al., 2018</xref>)</td>
<td align="center">2543</td>
<td align="center">1303 girls and 1240 boys</td>
<td align="center">7-12</td>
<td align="center">Record foot size through video capture system</td>
<td align="center">At 7-8 and 8&#x2013;9 years old for girls and 8&#x2013;9 and 10&#x2013;11 years old for boys, most measurements dramatically rose. The arch height, instep length and heel width of male and female had the largest increasing trend at the age of 7-12 years (P &#x3c; 0.05). Most of the sex differences occurred at ages 8, 9, and 11.</td>
<td align="center">In girls 7-8 and 8&#x2013;9 years old and boys 8&#x2013;9 and 10&#x2013;11 years old, the majority of measurements dramatically rose. For both sexes, ages 7 to 12 years, the largest increases were seen in arch height, instep length, and heel width.</td>
</tr>
<tr>
<td align="center">
<xref ref-type="bibr" rid="B17">Carvalho et al. (2017)</xref>
</td>
<td align="center">1394</td>
<td align="center">921 girls and 473 boys</td>
<td align="center">10-14</td>
<td align="center">determined weight, height, BMI, and FPI in the bipedal, static, and relaxed position.</td>
<td align="center">With the right foot, boys scored higher than girls.</td>
<td align="center">There were age differences between 11- and 13-year-old for the left foot. The 11-year-old group showed a greater tendency to pronate their feet.</td>
</tr>
<tr>
<td align="center">
<xref ref-type="bibr" rid="B69">Vrdoljak (2017)</xref>
</td>
<td align="center">2745</td>
<td align="center">1370 girls and 1375 boys</td>
<td align="center">2-7</td>
<td align="center">Six age categories were used to separate the population of kids. The length of the foot was measured using a measuring tape, while shape was determined clinically.</td>
<td align="center">In all age and sex groups, boys&#x27; and girls&#x27; left and right feet were identical in length and form.</td>
<td align="center">The second and third years were when the foot grow the fastest. The foot grow by around 1 cm a year from the third to the sixth year.</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>Remarks: Indicators and scoring standards for the FPI-6 test: (1) Foot posture indexes (FPI-6) Palpation of the talar head; (2) symmetry of the supra- and infra-lateral malleolar curvature; (3) position of the calcaneus in the frontal plane; (4) prominence near the talonavicular joint; (5) congruence of the medial longitudinal arch, and forefoot abduction or adduction on the rearfoot are other examination criteria. The total FPI-6 score ranged from -12 to 12, with each FPI-6 item being graded on a scale of -2 to 2. Based on their FPI-6 scores, the individuals were divided into three groups: 1) 0 to 5 is considered normal; 2) &#x3e;6 is considered pronated; 3) &#x3c; -1 is considered supinated (<xref ref-type="bibr" rid="B56">Redmond et al., 2008b</xref>).</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>2. Ball width is the x-y distance between points B1 and B2 projected; The distance between the instep and heel, measured horizontally, is known as the instep distance. Ball girth: the area around the forefoot that corresponds to the B1, B2, and BC points. (B2: fifth metatarsal; B1: first metatarsal; BC points: projected on the z-axis. This is shown in <xref ref-type="fig" rid="F2">Figure 2</xref>.)</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Illustration of Ball width (left) and Ball girth (right).</p>
</caption>
<graphic xlink:href="fbioe-11-1192524-g002.tif"/>
</fig>
<p>From the results in <xref ref-type="table" rid="T3">Table 3</xref>, (<xref ref-type="bibr" rid="B46">Mauch et al., 2008</xref>), concluded that flatfoot occurred at a higher rate in overweight children than in other normal weight and ultralight weight. Although a considerable number of studies have concluded that weight gain during growth can indirectly or directly cause flat feet, (e.g., plantar pressure due to weight gain and flattening of the MLA), the foot prosthesis could maintain the longitudinal arch through compensatory mechanisms (<xref ref-type="bibr" rid="B1">Aboelnasr et al., 2019</xref>). As the central nervous system matures in children, individuals would have better motor performance and balance. This would result in better control of lower limb posture (<xref ref-type="bibr" rid="B64">Swallen et al., 2005</xref>). Notably, the ossification of foot structures that accompanied skeletal development would allow the arch to remain stable under weight-bearing in children (<xref ref-type="bibr" rid="B8">athirgamanathan et al., 2019</xref>). External tibial rotation from the in-toe position at birth to the out-toe position during growth would result in a concomitant decrease in the morphology of the hindfoot exostosis (<xref ref-type="bibr" rid="B9">Atik and Ozyurek, 2014</xref>).</p>
<table-wrap id="T3" position="float">
<label>TABLE 3</label>
<caption>
<p>Influence of Obesity and Overweight on Foot Types</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">References</th>
<th align="center">Participants</th>
<th align="center">Age</th>
<th align="center">Category</th>
<th align="center">Method</th>
<th align="center">Result</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">
<xref ref-type="bibr" rid="B3">Agnieszka and Edyta, (2015)</xref>
</td>
<td align="center">207</td>
<td align="center">4-6</td>
<td align="center">OW</td>
<td align="center">Measurements included body weight, height, body mass index, and Clarke&#x27;s and gamma angles. Correlations between sex, nutritional health, and variations in foot arch height were also examined.</td>
<td align="center">The proportion of overweight and obese boys and girls increased between the ages of 4 and 6, and those with extra body weight tended to have collapsed medial longitudinal arches of the foot.</td>
</tr>
<tr>
<td align="center">
<xref ref-type="bibr" rid="B62">Stewart et al. (2018)</xref>
</td>
<td align="center">3713</td>
<td align="center">3-18</td>
<td align="center">OB</td>
<td align="center">Analysis of pediatric foot dimensions of children&#x27;s feet (foot length [FL] and foot width [FW])</td>
<td align="center">When compared to their obese counterparts, FL and FW were substantially shorter in male and female patients of normal weight.</td>
</tr>
<tr>
<td align="center">
<xref ref-type="bibr" rid="B46">Mauch et al. (2008)</xref>
</td>
<td align="center">2887</td>
<td align="center">2-14</td>
<td align="center">N, UW, OW</td>
<td align="center">Twelve relevant 3D foot measures were taken while the feet were in an upright bipedal position using a 3D foot scanner. The age, sex, height, and weight of the children were also recorded.</td>
<td align="center">Among underweight children, there was a larger percentage of thin feet (65-7%) compared to flat (4-50%), robust (89-100%), and short (21&#x2013;70%) feet. The disparities were considerably more obvious in the overweight kids. Age-related increases in robustness (69-337%) and flat feet (53-128%) were seen.</td>
</tr>
<tr>
<td align="center">
<xref ref-type="bibr" rid="B22">da Rocha et al. (2014)</xref>
</td>
<td align="center">40</td>
<td align="center">6-10</td>
<td align="center">N, OW</td>
<td align="center">Whether individuals were standing on one foot or two feet, the researchers measured the foot sensitivity and plantar pressure and compared the results between the feet and legs of obese and non-obese persons.</td>
<td align="center">Children who are overweight have fewer sensitive feet and more plantar pressure. In addition, sensitivity in various foot areas was comparable in obese and non-obese children.</td>
</tr>
<tr>
<td align="center">
<xref ref-type="bibr" rid="B34">Gijon-Nogueron et al. (2017)</xref>
</td>
<td align="center">1798</td>
<td align="center">6-12</td>
<td align="center">OW, OB</td>
<td align="center">Each had their height and weight assessed, and the body mass index (BMI) was computed. The foot posture is described using the foot posture index (FPI).</td>
<td align="center">Body mass does not appear to have a significant impact on static foot posture in children between the ages of 6 and 12.</td>
</tr>
<tr>
<td align="center">
<xref ref-type="bibr" rid="B37">Jimenez-Ormeno et al. (2013)</xref>
</td>
<td align="center">1032</td>
<td align="center">6-12</td>
<td align="center">N, OW, OB</td>
<td align="center">The body mass index was determined using measurements of height and weight. Obese, overweight, and normal-weight children were identified. An instatic, three-dimensional foot digitizer was used to measure the foot morphology.</td>
<td align="center">Overweight and obese kids develop bigger feet than their normal-weight peers.</td>
</tr>
<tr>
<td align="center">
<xref ref-type="bibr" rid="B27">Escalona-Marfil et al. (2022)</xref>
</td>
<td align="center">575</td>
<td align="center">5-10</td>
<td align="center">N, OW, OB, UW</td>
<td align="center">Foot posture and form evaluation (FPI) and body composition measurement</td>
<td align="center">The findings of this study show that children with normal weight, children who are overweight or obese, as well as children who are underweight, have different foot measurements (FPI, AHI, and MFW).</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>Remarks: 1. OW&#x3d;overweight; OB&#x3d;obeity; N&#x3d;normal; UW&#x3d;under weight</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>From the above analysis, it was clear that flatfoot may not be significantly correlated with changes in body mass index (<xref ref-type="bibr" rid="B35">Hawke et al., 2016</xref>; <xref ref-type="bibr" rid="B1">Aboelnasr et al., 2019</xref>). In other words, weight gain may not lead to flatfoot. (<xref ref-type="bibr" rid="B35">Hawke et al., 2016</xref>). found that children with greater internal rotation of the foot exhibited greater lower limb and overall body flexibility in a study of a sample of healthy asymptomatic children aged 7&#x2013;15&#xa0;years. Also, the findings of this study corroborated the discovery of a connection between flat feet and joint flexibility (<xref ref-type="bibr" rid="B51">Pfeiffer et al., 2006</xref>).</p>
</sec>
<sec id="s4-3">
<title>High-arch foot</title>
<p>Foot arch deformities were rarely seen in the early childhood population (under 3&#xa0;years of age). However, as children grow, the navicular bone, the final foot bone to ossify in children between the ages of two and five, was characterized by its fallibility and formative nature. As a result, it became a crucial consideration when evaluating the foot posture of four-year-old kids. Foot navicular ossification occurred later in boys than in girls, while the prevalence of pes cavus increased highly in boys between the period of 4 and 13 years, but the prevalence of pes cavus was frequent in the girl population (<xref ref-type="bibr" rid="B5">Alexander and Johnson, 1989</xref>; <xref ref-type="bibr" rid="B6">Aminian and Sangeorzan, 2008</xref>; <xref ref-type="bibr" rid="B75">Wozniacka et al., 2013</xref>; <xref ref-type="bibr" rid="B19">Chang et al., 2014</xref>).</p>
<p>Pes cavus was a common foot disorder in children while this disorder had an overall inversion of the foot, projection of the lateral edges of the foot, and inversion of the heel during standing (<xref ref-type="bibr" rid="B72">Wicart, 2012</xref>). This was generally caused by the deformity of pes cavus, which was cavus foot, a simple morphological feature but a normal variant often found in healthy individuals and growing children (<xref ref-type="bibr" rid="B5">Alexander and Johnson, 1989</xref>; <xref ref-type="bibr" rid="B58">Schwend and Drennan, 2003</xref>; <xref ref-type="bibr" rid="B19">Chang et al., 2014</xref>). While the other condition was direct cavus foot, which was the result of foot deformity and often only affected the sagittal plane (forefoot, hindfoot, or both) occurred only in the sagittal plane (forefoot, hindfoot, or both). Direct cavus foot may be associated with multiple causes, and several studies have shown that the condition was due to structural problems in the brain, spinal cord, peripheral nerves, or foot, while neurological disorders were seen primarily in the posterior cavus foot (<xref ref-type="bibr" rid="B58">Schwend and Drennan, 2003</xref>; <xref ref-type="bibr" rid="B72">Wicart, 2012</xref>). CMT was the most common neurologically caused disorder in this condition (<xref ref-type="bibr" rid="B16">Burns et al., 2009</xref>). The risk of deterioration in childhood can generally be averted with the right conservative care (orthotic realignment of the foot) (<xref ref-type="bibr" rid="B72">Wicart, 2012</xref>).</p>
</sec>
</sec>
<sec sec-type="discussion" id="s5">
<title>Discussion</title>
<sec id="s5-1">
<title>Influence of sex and age differences</title>
<p>Changes in foot morphology in children were gradual over time, particularly the growth of foot length and width. The critical age for foot development was 6&#xa0;years, and (<xref ref-type="bibr" rid="B71">Waseda et al., 2014</xref>). found that children&#x2019;s foot length increased rapidly from the age of 6&#xa0;years. Changes in foot morphology characteristics were minimal during the age interval of 10&#x2013;11&#xa0;years and stabilized at 12&#xa0;years (<xref ref-type="bibr" rid="B21">Cheng et al., 1997</xref>; <xref ref-type="bibr" rid="B26">El et al., 2006</xref>; <xref ref-type="bibr" rid="B18">Catan et al., 2020</xref>). Cheng et al. (<xref ref-type="bibr" rid="B21">Cheng et al., 1997</xref>) found that children&#x2019;s foot length and width increased by an average of 8&#x2013;10&#xa0;mm per year between the ages of 6&#x2013;12&#xa0;years. (<xref ref-type="bibr" rid="B48">Muller et al., 2012</xref>). reported that the length and width of the foot grew with age, it was demonstrated that the growth rate of foot length practically hit a plateau at 13&#xa0;years for girls and 14&#xa0;years for boys at that point (<xref ref-type="bibr" rid="B29">Evans et al., 2012</xref>; <xref ref-type="bibr" rid="B71">Waseda et al., 2014</xref>).</p>
<p>In terms of sex differences, the change in the foot was comparable, however, there could be variations between 8 and 10&#xa0;years old (<xref ref-type="bibr" rid="B25">Delgado-Abellan et al., 2014</xref>). According to (<xref ref-type="bibr" rid="B21">Cheng et al., 1997</xref>), until the age of 3 years, variations in foot length and width in males were comparable to those in girls. Boys&#x2019; feet development increased after the age of 3 years. At the age of 9, boys and girls showed considerable disparities, according to research by Bosch, Gerss, and Rosenbaum (<xref ref-type="bibr" rid="B11">Bosch et al., 2010</xref>). Nevertheless, no information regarding foot length was provided in this investigation. (<xref ref-type="bibr" rid="B61">Stavlas et al., 2005</xref>). found that the average annual foot length growth rate was 4.3% for boys and 3.9% for girls. The study also revealed that the fastest growth rates were observed at ages 8-9 and 10-11 for boys, and ages 7-8 and 8-9 for girls. Thus, peak growth rates occur earlier in girls than in boys. The age of 7&#x2013;12&#xa0;years was the stage of rapid growth in foot arch height among Chinese boys and girls. Studies showed that the navicular height of boys&#x2019; feet would increase from 6 to 13&#xa0;years of age (<xref ref-type="bibr" rid="B65">Szczepanowska-Wolowiec et al., 2021</xref>). The navicular or talar navicular joint line was often used to determine the height of medial longitudinal arch. Between the ages of 8 and 13, the arch height of girls rose. The arch height ratio in boys was practically flat until age 11 but considerably rose from age 11 to 13. The formula for the arch height ratio is AHR (%) &#x3d; navicular height&#x2a;100/foot length. Girls&#x2019; arch height ratios were largely flat until age 10 but considerably rose between age 10 and 12.</p>
<p>Foot morphology changed with growth and development. (<xref ref-type="bibr" rid="B7">Ana et al., 2017</xref>). performed the Foot Posture Index (FPI) test for both feet among 2,569 children aged 9&#x2013;15&#xa0;years during 2016&#x2013;2018. The FPI was a clinical diagnostic tool designed to quantify the grade of foot position (posture), such as neutral, internally rotated, or posteriorly rotated. The index was developed using a simple six-factor method to assess foot morphology, to obtain simple and quantitative postures (<xref ref-type="bibr" rid="B4">Al Kaissi et al., 2016</xref>). It was reported that girls had a higher percentage of rotated feet than boys, and boys presented higher FPI-6 scores than girls, suggesting that boys had flatter feet and that children and adolescents aged 9&#x2013;15&#xa0;years had neutral or mildly internally rotated foot morphology. (<xref ref-type="bibr" rid="B36">Heidi and Priv, 2015</xref>). conducted a study on foot morphology in infants who just started walking independently. The study showed that boys&#x2019; feet were flatter and had a lower arch than girls&#x2019; feet, indicating that males were more likely than girls to have higher FPI-6 scores from an early age.</p>
<p>In other words, the effect of sex differences on foot morphology may be present since birth, and such a condition may exist during growth. The effect of age differences on the foot was also presented from the time of birth, and because of the age difference, the foot width and length grew at different rates, which was a dynamic process. (<xref ref-type="bibr" rid="B4">Al Kaissi et al., 2016</xref>). observed differences between children and adult populations, with children generally presenting a neutral foot and internally rotated foot stance, and (<xref ref-type="bibr" rid="B73">Wilkerson and Mason, 2000</xref>) found that adults generally presented a neutral foot stance. The study discovered that with increased muscle mass, myelination of motor neurons, and subsequently enhanced muscular strength from puberty forward, the medial longitudinal arch (MLA) had stronger support. This function would contribute to the development of a neutral foot.</p>
<p>In studies of normal foot type, characteristics of foot morphology could be evaluated by footprint, foot index, FPI, manual measurement, and camera acquisition. A large sample of data and studies reported (<xref ref-type="bibr" rid="B5">Alexander and Johnson, 1989</xref>; <xref ref-type="bibr" rid="B6">Aminian and Sangeorzan, 2008</xref>; <xref ref-type="bibr" rid="B36">Heidi and Priv, 2015</xref>; <xref ref-type="bibr" rid="B35">Hawke et al., 2016</xref>; <xref ref-type="bibr" rid="B27">Escalona-Marfil et al., 2022</xref>) that incorrect gait and walking postures and related external factors were the causes of foot disorders in children.</p>
</sec>
<sec id="s5-2">
<title>Influence of body weight variations</title>
<p>Apart from the above factors of age and sex, variations in body weight and height could also lead to changes in the biological structure of the foot (<xref ref-type="bibr" rid="B71">Waseda et al., 2014</xref>; <xref ref-type="bibr" rid="B10">Bailly et al., 2022</xref>). Being overweight has implications for foot structure, including alterations of anatomical structure, abnormalities in plantar pressure distribution, and balance (<xref ref-type="bibr" rid="B14">Bruner et al., 2009</xref>; <xref ref-type="bibr" rid="B71">Waseda et al., 2014</xref>; <xref ref-type="bibr" rid="B44">Manousaki et al., 2019</xref>; <xref ref-type="bibr" rid="B10">Bailly et al., 2022</xref>). BMI is a popular tool for assessing overweight and obesity as a straightforward measure of the connection between weight and height. The overweight individuals have higher ratios of arch collapse due to thicker layers of adipose tissue (<xref ref-type="bibr" rid="B64">Swallen et al., 2005</xref>). Medial section of the plantar foot in a group of 8-year-old children had denser adipose tissue, and the height of longitudinal arch was lower in these observations (<xref ref-type="bibr" rid="B73">Wilkerson and Mason, 2000</xref>). (<xref ref-type="bibr" rid="B3">Agnieszka and Edyta, 2015</xref>) found that being overweight had a negative effect on the longitudinal arch in preschool children. In preschoolers, no correlation between BMI and the height of the transverse arch was found, but in preschoolers of normal weight, the height of longitudinal arch was significantly increased. In contrast, a trend towards the decreasing longitudinal arch height in overweight and obese boys and girls was found. (<xref ref-type="bibr" rid="B22">da Rocha et al., 2014</xref>). concluded that foot sensitivity was lower in obese children than non-obese children. Obese children showed similar sensitivity in all foot regions, while non-obese children were able to differentiate the intensities of touch on different regions. Studies showed that higher sensitivity to touch was associated with higher receptor density, which decreased with age. Therefore, the lower sensitivity in obese children may be due to lower receptor density per surface area unit (<xref ref-type="bibr" rid="B38">Koz&#x142;owska, 1988</xref>), but this is only theory at this time, and no particular experimental verification of this assumption has been carried out. Future studies may consider examining the receptor density of foot surface area in obese, overweight, normal, and ultralight children as per age group and BMI groups. (<xref ref-type="bibr" rid="B40">Lee et al., 2013</xref>).</p>
<p>Overweight boys during childhood may have bigger feet, indicating that obesity may be a major factor affecting foot growth (as determined by the size recorded in the available data set). The structural characteristics of the foot in obese children were wider and thicker, which may increase the peak plantar pressure and vertical peak pressure during gait. Lower footprint angle (FA), higher Chippaux-Smirak index (CSI), higher plantar pressure (<xref ref-type="bibr" rid="B43">Lobstein and Frelut, 2003</xref>), higher arch index (AI), and greater footprint area (<xref ref-type="bibr" rid="B63">Stovitz et al., 2008</xref>) were found in obese children feet. Children with high body weight may show less degree of variations in the foot morphology or the changes might be gradual or subtle. Thus, (<xref ref-type="bibr" rid="B37">Jimenez-Ormeno et al., 2013</xref>), suggested that being overweight may be an important factor affecting foot development in prepubescent students at school. (<xref ref-type="bibr" rid="B46">Mauch et al., 2008</xref>). found that low percentage of flatfoot was observed in underweight children. However, the likelihood of flat feet rises with age, although this is highly documented in overweight children.</p>
<p>Obesity would lead to the compensation of foot arch, and either indirectly or directly contribute to the development of flat feet (<xref ref-type="bibr" rid="B57">Sachithanandam and Joseph, 1995</xref>; <xref ref-type="bibr" rid="B20">Chen et al., 2013</xref>; <xref ref-type="bibr" rid="B60">Song-Hua et al., 2017</xref>; <xref ref-type="bibr" rid="B15">Buldt et al., 2018</xref>; <xref ref-type="bibr" rid="B67">Telfer and Bigham, 2019</xref>). However, a recent study of 728 children between 3 and 15 years old found a relationship between weight and foot morphology (<xref ref-type="bibr" rid="B28">Evans and Karimi, 2015</xref>). While Evans (<xref ref-type="bibr" rid="B28">Evans and Karimi, 2015</xref>) refuted that heavier children had flatter feet, and further emphasized no association between increased body weight and flatfeet among children. Whilst this statement contradicted with several studies (<xref ref-type="bibr" rid="B57">Sachithanandam and Joseph, 1995</xref>; <xref ref-type="bibr" rid="B43">Lobstein and Frelut, 2003</xref>; <xref ref-type="bibr" rid="B20">Chen et al., 2013</xref>; <xref ref-type="bibr" rid="B67">Telfer and Bigham, 2019</xref>), which may be a convergent prediction of the foot morphology in overweight and obese children. Currently, weight reduction was not employed as a treatment in the traditional treatment of flat feet due to obesity. Therefore, it was suggested that further follow-up studies should be conducted focusing on this issue. Yet, alterations in foot morphology brought on by excess weight may cause discomfort or pain and may increase reluctance to exercise, which might result in body weight growth. Considering the development of healthy children, increased attention is still required, especially for physical activity and diet control.</p>
</sec>
<sec id="s5-3">
<title>Abnormal foot type</title>
<sec id="s5-3-1">
<title>Pes planus (flat foot)</title>
<p>The influence of weight, sex, and age was discussed for the development of flat feet. (<xref ref-type="bibr" rid="B29">Evans et al., 2012</xref>). found that between the age of 5&#x2013;10&#xa0;years, girls had higher arches than boys. (<xref ref-type="bibr" rid="B7">Ana et al., 2017</xref>). investigated 2,569 Japanese kids between the age of 9&#x2013;15 using the FPI-6, discovering that kids exhibited neutral or moderate internal rotation in standing posture, with a mean score of 3&#x2013;3.4. Based on a sample of 140 children aged 7&#x2013;10&#xa0;years, (<xref ref-type="bibr" rid="B1">Aboelnasr et al., 2019</xref>), used FPI-6 screening to identify a sample of 31 kids with flat feet. Basic anthropometric measurements were compared between subjects designated with flat feet, reporting that waist size was associated with foot morphology (although not significantly), but conversely, a &#x201c;fatter&#x201d; waist was less associated with flat feet. In other words, weight gain and flat feet were unrelated. In a study by (<xref ref-type="bibr" rid="B35">Hawke et al., 2016</xref>), basic data on 30 healthy, asymptomatic kids aged 7 to 15 were gathered, including height and weight (BMI), Beighton score, Foot Posture Index-6 (FPI), and lower extremity evaluation. A correlation between flat feet and joint flexibility was discovered, and internal foot rotation was associated with lower limb and overall body flexibility in healthy and asymptomatic children, but not related with the ankle flexibility (<xref ref-type="bibr" rid="B1">Aboelnasr et al., 2019</xref>), which was consistent with a previous statement (<xref ref-type="bibr" rid="B35">Hawke et al., 2016</xref>). This finding supported that neutral and internally rotated foot postures predominated over other foot postures, as reported by Evans (<xref ref-type="bibr" rid="B29">Evans et al., 2012</xref>) that being overweight would not cause flat feet.</p>
<p>The current review discussed flatfoot based on asymptomatic participants, focusing on the effect of growth and development on the biological shape of the children foot and the potential cause of flatfoot.</p>
</sec>
<sec id="s5-3-2">
<title>Pes cavus (high arch)</title>
<p>Cavus foot was used to describe the foot type that had high arch as a typical characteristic. High arch may be caused by a high pitch angle in the hindfoot, hyperflexion of the plantar aspect in the forefoot, or hyperflexion of the midfoot. In complex cases, the cavus foot may be driven by a narrow pitch-heel angle and a possible torsional component in the midfoot. The components of the venous cavity showed increased pronation and pitch of the hindfoot, plantar flexion of the midfoot, and pronation and inversion of the forefoot. The shape of the foot cavity is associated with changes in foot mechanics.</p>
<p>(<xref ref-type="bibr" rid="B5">Alexander and Johnson, 1989</xref>) stated that arch deformities were rarely observed in young children (under 3 years) but may occur as children grow. The etiology could be attributed to problems in the brain, spinal cord, peripheral nerves, or foot structure. When motor imbalances occurred before skeletal maturation, the healthy bone morphology may result in substantial changes. When cavernous cavities were acquired after skeletal maturation, there may be little or no change in foot morphology. Two-thirds of adults with symptomatic cavus foot have an underlying neurological condition. CMT disease was the most prevalent. The findings of (<xref ref-type="bibr" rid="B75">Wozniacka et al., 2013</xref>) indicated that a high prevalence of high arched feet. Those with symptomatic cavus feet were two-thirds more likely to have a neurological disorder. The most common disease among children and teenagers between the ages of 4 and 13 was the CMT disease. On the right foot, 66.5% of children had high arches, compared to 61.4% on the left, and girls were more likely to have high arches than boys. (<xref ref-type="bibr" rid="B19">Chang et al., 2014</xref>). studied static foot morphology, including foot navicular height and arch volume during sitting and standing in 27 children aged 2&#x2013;6&#xa0;years. The study found that the arch volume index (AVI) was significantly correlated with pressure changes in the midfoot (<xref ref-type="bibr" rid="B63">Stovitz et al., 2008</xref>), which implied that AVI measured in the static position could be correlated with dynamic changes in mid-foot lower-foot loading. However, there was no correlation between AVI and mean pressure and force throughout the stance phase (<xref ref-type="bibr" rid="B29">Evans et al., 2012</xref>). As the arch height decreasing, the pressure and force on the medial metatarsal and midfoot plantar increased (<xref ref-type="bibr" rid="B68">Villarroya et al., 2009</xref>). Compared with NH, the correlation between arch volume and foot pressure distribution is higher, so the cause of high arch formation may come from changes in foot structure (<xref ref-type="bibr" rid="B52">Putti et al., 2010</xref>). Foot structure may alter over time because of weight fluctuations, foot growth, and development, which could eventually cause musculoskeletal disease to manifest.</p>
<p>The studies included in the current review were based on asymptomatic participants, comparing to the different foot types and those asymptomatic individuals who seem healthy but have higher risks of musculoskeletal diseases.</p>
</sec>
</sec>
</sec>
<sec sec-type="conclusion" id="s6">
<title>Conclusion</title>
<p>This review study mainly investigated three issues, including (1) how age and sex variations affect changes in foot morphology, (2) the effect of weight changes on foot morphology, and (3) common abnormal foot morphology during the growth and development of children. Key finding of this review was that sex, age, and weight change would affect foot size, bony structure, foot posture, and plantar pressures during childhood. As per this biological nature, children feet generally exhibit neutral and internally rotated foot postures, which frequently contribute to abnormal foot morphologies (e.g., flat feet and high-arched feet).</p>
<p>This review comprehensively synthesized several published evidence in previous studies, while future studies may consider focusing on the contribution of other factors to specific foot shapes during child development (in addition to the studies presented here) and further expand the information of the research and application of foot morphologies and conditions in children, thus providing comprehensive knowledge for healthy children development.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="s7">
<title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding author.</p>
</sec>
<sec id="s8">
<title>Author contributions</title>
<p>Conceptualization: HJ, QM, and YG; methodology: HJ, QM, YW, JH, and ES; writing&#x2014;original draft preparation: HJ, QM, YW, and ES; writing&#x2014;review and editing: JF and YG; supervision: QM and YG; project administration: QM and YG; funding acquisition: QM and YG. All authors contributed to the article and approved the submitted version.</p>
</sec>
<sec id="s11">
<title>Funding</title>
<p>This study was supported by the National Natural Science Foundation of China (No. 12202216), Ningbo Natural Science Foundation, Ningbo University Teaching and Research project (JYXM2023051), SRIP project of Ningbo University (No. 2023SRIP0501, No. 2023SRIP0510 and No. 2023SRIP0502) and K. C. Wong Magna Fund in Ningbo University.</p>
</sec>
<sec sec-type="COI-statement" id="s9">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="disclaimer" id="s10">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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